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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 233193Erstellt: 24. Oktober 2026

p-Bromoacetophenone → 4-Bromo-1-(1,3-dithian-2-yl)ethylbenzene

https://huagongshe.com/de/reaction/233193

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-BromoacetophenoneHCID 7466—
EduktBoron trifluoride etherateHCID 8000—
Edukt1,3-PropanedithiolHCID 8013—
LösungsmittelChloroformHCID 6212—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Bromo-1-(1,3-dithian-2-yl)ethylbenzeneHCID 21960112—

Reaktionsschritte

To the compound p-bromoacetophenone (36.85 g, 185 mmol) in trichloromethane (300 ml) was added 1,3-propanedithiol (25 g, 230 mmol) and boron trifluoride etherate (3 ml). The resulting mixture was stirred at room temperature for 48 hours. The mixture was diluted with dichloromethane (500 ml), washed twice with 10% sodium hydroxide (200 ml), water, and brine, and then dried (Na2SO4). The product was concentrated to an oil. A portion was stirred with ether (100 ml) and a crystalline product was formed. The crystalline product was recovered by filtration and purified by recrystallization to yield 4-bromo-1-(1,3-dithian-2-yl)ethylbenzene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05591745
Quelldatensatzuspto-grants-1997_01
ORD IDord-9c1cde608ff74529a27e9527933d49c7
Quellennotizuspto-grants-1997_01